ClinVar Miner

List of variants in gene SCN8A reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 101
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HGVS dbSNP
NM_014191.4(SCN8A):c.*8C>T rs1057520364
NM_014191.4(SCN8A):c.-55+13A>G rs1555205506
NM_014191.4(SCN8A):c.-55+20C>G rs926099486
NM_014191.4(SCN8A):c.-61C>T rs1032376116
NM_014191.4(SCN8A):c.1002A>G (p.Pro334=) rs1057520362
NM_014191.4(SCN8A):c.1104C>A (p.Thr368=) rs371872378
NM_014191.4(SCN8A):c.1135-13T>C rs1057520363
NM_014191.4(SCN8A):c.1173C>T (p.Phe391=) rs886049582
NM_014191.4(SCN8A):c.1204C>T (p.Leu402=) rs1057522082
NM_014191.4(SCN8A):c.1342-18C>T rs763911558
NM_014191.4(SCN8A):c.1424G>A (p.Arg475Gln) rs201018451
NM_014191.4(SCN8A):c.1545G>T (p.Val515=) rs779561924
NM_014191.4(SCN8A):c.1591C>T (p.Leu531=) rs773176178
NM_014191.4(SCN8A):c.1635+102G>A
NM_014191.4(SCN8A):c.1636-16del rs754973942
NM_014191.4(SCN8A):c.1677C>T (p.His559=) rs202212399
NM_014191.4(SCN8A):c.1686G>A (p.Lys562=) rs764350935
NM_014191.4(SCN8A):c.1717C>A (p.Arg573=) rs370074236
NM_014191.4(SCN8A):c.1770G>A (p.Thr590=) rs773379793
NM_014191.4(SCN8A):c.1779G>C (p.Glu593Asp) rs760717246
NM_014191.4(SCN8A):c.1818G>C (p.Arg606=) rs777424314
NM_014191.4(SCN8A):c.1846_1854GGCTACAGC[3] (p.616_618GYS[3])
NM_014191.4(SCN8A):c.1908C>T (p.Ser636=) rs1053543226
NM_014191.4(SCN8A):c.2073C>T (p.Tyr691=) rs146982102
NM_014191.4(SCN8A):c.2109T>C (p.Val703=) rs369029348
NM_014191.4(SCN8A):c.2131+26A>C
NM_014191.4(SCN8A):c.2371-17T>G rs1193837480
NM_014191.4(SCN8A):c.2545-4T>G rs1175986621
NM_014191.4(SCN8A):c.2586C>T (p.Asn862=) rs377396450
NM_014191.4(SCN8A):c.2616G>T (p.Val872=) rs778358285
NM_014191.4(SCN8A):c.2685A>G (p.Gln895=) rs528126331
NM_014191.4(SCN8A):c.277-23TC[2] rs765408317
NM_014191.4(SCN8A):c.3024G>A (p.Val1008=) rs1057521309
NM_014191.4(SCN8A):c.3060G>A (p.Gln1020=) rs528718802
NM_014191.4(SCN8A):c.3090G>A (p.Glu1030=) rs1057523246
NM_014191.4(SCN8A):c.3135C>T (p.Ile1045=) rs550579591
NM_014191.4(SCN8A):c.3147C>T (p.Thr1049=) rs567527548
NM_014191.4(SCN8A):c.3148G>A (p.Gly1050Ser) rs202006479
NM_014191.4(SCN8A):c.3321C>T (p.Asn1107=) rs374213514
NM_014191.4(SCN8A):c.3327C>T (p.Asn1109=) rs1349215930
NM_014191.4(SCN8A):c.3372+62C>G
NM_014191.4(SCN8A):c.3408C>T (p.Thr1136=) rs1555226263
NM_014191.4(SCN8A):c.3423A>G (p.Pro1141=) rs376102810
NM_014191.4(SCN8A):c.3459A>G (p.Glu1153=) rs1057522632
NM_014191.4(SCN8A):c.3491-12C>T rs369532655
NM_014191.4(SCN8A):c.3643C>T (p.Leu1215=) rs532528307
NM_014191.4(SCN8A):c.3645+112G>A
NM_014191.4(SCN8A):c.3645+14G>C rs202031360
NM_014191.4(SCN8A):c.3645+19T>G rs1057521948
NM_014191.4(SCN8A):c.3669G>A (p.Glu1223=) rs1318771897
NM_014191.4(SCN8A):c.3738G>A (p.Glu1246=) rs376953145
NM_014191.4(SCN8A):c.3819+13C>G rs754542157
NM_014191.4(SCN8A):c.3819+34C>G
NM_014191.4(SCN8A):c.3943-17C>G rs1057523298
NM_014191.4(SCN8A):c.395+327G>A
NM_014191.4(SCN8A):c.3957C>T (p.Ala1319=) rs764790057
NM_014191.4(SCN8A):c.396-5T>C rs764928471
NM_014191.4(SCN8A):c.3999G>A (p.Val1333=) rs796053208
NM_014191.4(SCN8A):c.402T>C (p.Phe134=) rs559668426
NM_014191.4(SCN8A):c.4227+225G>A
NM_014191.4(SCN8A):c.4282-233C>T
NM_014191.4(SCN8A):c.4350C>T (p.Phe1450=) rs753234714
NM_014191.4(SCN8A):c.4359C>T (p.Phe1453=) rs746544103
NM_014191.4(SCN8A):c.435C>T (p.Asn145=) rs1057522588
NM_014191.4(SCN8A):c.4420-119A>G
NM_014191.4(SCN8A):c.4446C>T (p.Thr1482=) rs374059983
NM_014191.4(SCN8A):c.4725G>A (p.Ala1575=) rs756326813
NM_014191.4(SCN8A):c.4748T>C (p.Ile1583Thr) rs201458257
NM_014191.4(SCN8A):c.474G>A (p.Ser158=) rs374989727
NM_014191.4(SCN8A):c.4764C>T (p.Phe1588=) rs200728478
NM_014191.4(SCN8A):c.485+17T>C rs748436294
NM_014191.4(SCN8A):c.485+18G>A rs369368623
NM_014191.4(SCN8A):c.492G>A (p.Thr164=) rs762641381
NM_014191.4(SCN8A):c.4969C>T (p.Leu1657=) rs374755275
NM_014191.4(SCN8A):c.5046C>T (p.Ile1682=) rs376759643
NM_014191.4(SCN8A):c.5118T>C (p.Gly1706=) rs776753024
NM_014191.4(SCN8A):c.5229C>A (p.Ile1743=) rs370268493
NM_014191.4(SCN8A):c.5232C>T (p.Phe1744=) rs1555231003
NM_014191.4(SCN8A):c.5265A>G (p.Leu1755=) rs1555231005
NM_014191.4(SCN8A):c.5271C>T (p.Val1757=) rs752174650
NM_014191.4(SCN8A):c.5385C>T (p.Phe1795=) rs748215769
NM_014191.4(SCN8A):c.5403G>A (p.Gln1801=) rs1555231039
NM_014191.4(SCN8A):c.5472C>G (p.Pro1824=) rs60637
NM_014191.4(SCN8A):c.5577C>T (p.Ser1859=) rs185667241
NM_014191.4(SCN8A):c.5580G>A (p.Gly1860=) rs201484402
NM_014191.4(SCN8A):c.5619C>T (p.Phe1873=)
NM_014191.4(SCN8A):c.579A>G (p.Pro193=) rs755900174
NM_014191.4(SCN8A):c.5841T>C (p.Tyr1947=)
NM_014191.4(SCN8A):c.615-189C>T
NM_014191.4(SCN8A):c.706+13G>A rs376385273
NM_014191.4(SCN8A):c.707-15A>G rs149586118
NM_014191.4(SCN8A):c.726T>A (p.Gly242=) rs779319824
NM_014191.4(SCN8A):c.744G>A (p.Val248=) rs201298141
NM_014191.4(SCN8A):c.768C>A (p.Ile256=) rs1231477580
NM_014191.4(SCN8A):c.804C>T (p.Ile268=) rs375241678
NM_014191.4(SCN8A):c.814C>T (p.Leu272=) rs769727012
NM_014191.4(SCN8A):c.858A>T (p.Ile286=) rs370911858
NM_014191.4(SCN8A):c.867C>T (p.Asn289=) rs375801783
NM_014191.4(SCN8A):c.928+164T>C
NM_014191.4(SCN8A):c.992+10T>A rs367746278
NM_014191.4(SCN8A):c.996A>G (p.Gln332=) rs1057522020

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